Canonical Allele Identifier: CA452990126

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470062T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148928T>C , CM000668.2:g.157148928T>C	GRCh38
NC_000006.11:g.157470062T>C , CM000668.1:g.157470062T>C	GRCh37
NC_000006.10:g.157511754T>C	NCBI36
NG_032093.1:g.375999T>C
NG_032093.2:g.375999T>C
NG_066624.1:g.377903T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3066T>C	ENSP00000055163.8:p.Ala1022=
ENST00000414678.8:c.2976T>C	ENSP00000412835.3:p.Ala992=
ENST00000637015.2:c.3066T>C	ENSP00000489729.2:p.Ala1022=
ENST00000319584.11:c.1080T>C	ENSP00000313006.7:p.Ala360=
ENST00000346085.10:c.3105T>C	ENSP00000344546.5:p.Ala1035=
ENST00000350026.10:c.2817T>C	ENSP00000055163.7:p.Ala939=
ENST00000414678.7:c.1224T>C	ENSP00000412835.2:p.Ala408=
ENST00000452544.2:n.967T>C
ENST00000635849.1:c.387T>C	ENSP00000490948.1:p.Ala129=
ENST00000635957.1:c.21T>C	ENSP00000490385.1:p.Ala7=
ENST00000636426.1:n.200T>C
ENST00000636930.2:c.3066T>C MANE Select	ENSP00000490491.2:p.Ala1022=
ENST00000637015.1:c.305T>C
ENST00000637568.1:c.109T>C
ENST00000637810.1:c.567T>C	ENSP00000489636.1:p.Ala189=
ENST00000637904.1:c.567T>C	ENSP00000490550.1:p.Ala189=
ENST00000647938.1:c.2856T>C	ENSP00000498155.1:p.Ala952=
ENST00000674190.1:n.1815T>C
ENST00000319584.10:c.1083T>C	ENSP00000313006.6:p.Ala361=
ENST00000346085.9:c.2856T>C	ENSP00000344546.4:p.Ala952=
ENST00000350026.9:c.2817T>C	ENSP00000055163.7:p.Ala939=
ENST00000400790.3:c.18T>C	ENSP00000383596.3:p.Ala6=
ENST00000414678.6:c.1224T>C	ENSP00000412835.2:p.Ala408=
ENST00000452544.1:n.913T>C
ENST00000478761.3:c.139T>C
NM_017519.2:c.2817T>C	NP_059989.2:p.Ala939=
NM_020732.3:c.2856T>C	NP_065783.3:p.Ala952=
XM_005267069.3:c.2817T>C	XP_005267126.2:p.Ala939=
XM_011535984.1:c.1767T>C	XP_011534286.1:p.Ala589=
XM_011535985.1:c.1587T>C	XP_011534287.1:p.Ala529=
XM_011535986.1:c.1347T>C	XP_011534288.1:p.Ala449=
XM_011535987.1:c.966T>C	XP_011534289.1:p.Ala322=
XM_011535988.1:c.-20+15721T>C	XP_011534290.1:n.-20+15721T>C
NM_001346813.1:c.2817T>C	NP_001333742.1:p.Ala939=
NM_001363725.1:c.567T>C	NP_001350654.1:p.Ala189=
XM_011535984.2:c.2898T>C	XP_011534286.2:p.Ala966=
XM_011535988.3:c.-20+15721T>C	XP_011534290.1:n.-20+15721T>C
XM_017011103.2:c.2898T>C	XP_016866592.1:p.Ala966=
XM_017011104.1:c.2898T>C	XP_016866593.1:p.Ala966=
XM_017011105.2:c.2898T>C	XP_016866594.1:p.Ala966=
XM_017011106.2:c.2898T>C	XP_016866595.1:p.Ala966=
XM_017011107.2:c.2718T>C	XP_016866596.1:p.Ala906=
XR_002956289.1:n.2981T>C
NM_001363725.2:c.567T>C	NP_001350654.1:p.Ala189=
NM_001371656.1:c.3105T>C	NP_001358585.1:p.Ala1035=
NM_001374820.1:c.3105T>C	NP_001361749.1:p.Ala1035=
NM_001374828.1:c.3066T>C MANE Select	NP_001361757.1:p.Ala1022=
NM_017519.3:c.3066T>C	NP_059989.3:p.Ala1022=